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Diffusion Tensor Imaging in Cubital Tunnel Syndrome
Ryckie George Wade1, Timothy T Griffiths1, Robert Flather1, Irvin Teh1, Hamied A Haroon2, David Shelley3, Sven Plein1, and Grainne Bourke3
1University of Leeds, Leeds, United Kingdom, 2University of Manchester, Manchester, United Kingdom, 3Leeds Teaching Hospitals, Leeds, United Kingdom

Synopsis

Cubital Tunnel Syndrome (CuTS) is the 2nd most common compressive neuropathy affecting 6% of the population. Surgical decompression is the most effective treatment, but clinicians lack a reliable test to select patients for surgery. Diffusion tensor imaging (DTI) characterises tissue microstructure and so, DTI was acquired from 14 controls and 8 patients awaiting surgery in this proof-of-concept study. Patients had a significantly lower FA and higher RD than controls, throughout the length of the ulnar nerve. Therefore, DTI may add objective evidence of the ‘health’ of the ulnar nerve and aid the management of cubital tunnel syndrome.

Introduction

Cubital Tunnel Syndrome (CuTS) is the 2nd most common compressive neuropathy, affecting 36 per 100,000 person years[1] or 6% of the population[2]. Chronic compression leads to distortion of the axonal architecture, demyelination and fibrosis[3,4]. Surgical decompression is the most effective treatment and approximately 15,000 people per annum undergo surgical decompression in the UK[5] and USA[6]. However, clinicians lack a reliable test to select patients for surgery[7,8] and consequently, surgical decompression is unbeneficial in 13% of patients[9]. Furthermore, there is no non-invasive test which can objectively assess the ‘health’ of the ulnar nerve after surgery.[10] Diffusion tensor imaging (DTI) characterises tissue microstructure and provides reproducible[11–14] proxy measures of nerve ‘health’ which are sensitive to myelination, axon diameter, fibre density and organisation[15,16]. This study investigates the differences in the DTI metrics of the ulnar nerve between asymptomatic adults and those with CuTS (awaiting surgery).

Methods

Asymptomatic adults and consecutive patients with a recent diagnosis of CuTS who were scheduled for decompressive surgery in our institution were recruited between July and November 2019. DTI was acquired at 3.0 tesla using single-shot echo-planar imaging (55 axial slices, 3 mm thick, 1.5 mm2 in-plane) with 30 diffusion sensitising gradient directions, a b-value of 800 s/mm2 and 4 signal averages. The sequence was repeated with the phase-encoding direction reversed. Data were combined and corrected in FSL[17] and imported to DSI Studio. Diffusion was quantified using restricted diffusion imaging[18] and reconstructed using generalised q-sampling imaging[19] (Figure 1). From every slice, the fractional anisotropy (FA), normalised quantitative anisotropy (nQA), mean diffusivity (MD), axial diffusivity (AD) and radial diffusivity (RD) were extracted from 3 mm2 regions of interest covering the ulnar nerve. Metrics between patients with CuTS and controls were compared using mixed-effects linear regression.

Results

Thirteen controls (8 males, 5 females) and 8 patients with CuTS (6 males, 2 females) completed the study. Patients had a significantly lower FA than controls (mean difference 0.031 [95% CI 0.014, 0.048]; Figure 2) with the largest disparity in the arm (mean difference 0.087 [95% CI 0.035, 0.141]). Patients also had a significantly higher RD through the length of the ulnar nerve than controls (mean difference 0.252 [95% CI 0.085, 0.419]) with the largest disparity observed in the forearm (mean difference 0.252 x 10-4 mm2/s [95% CI 0.085 x 10-4, 0.419 x10-4]; Figure 3). There were no significant differences between patients and controls in QA, MD or AD. There was strong agreement between raters (ICC 0.02 [95% CI 0.002, 0.11]) as the variance in FA due to the person performing the analysis was 0.005 (95% CI 0.002, 0.01).

Conclusions

This study shows that some diffusion tensor imaging metrics of the ulnar nerve in adults with CuTS are significantly different to those of asymptomatic adults. Moreover, these differences appear to manifest throughout the length of the ulnar nerve, not just at the supposed site of compression within the cubital tunnel. These findings suggest that DTI may add objective evidence of the ‘health’ of the ulnar nerve and aid in the management of cubital tunnel syndrome.

Acknowledgements

No acknowledgement found.

References

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Figures

Figure 1. Data derived from a healthy control. The rows show data from the arm, cubital tunnel and forearm. The columns contain T2-weighted scans, and corresponding maps of normalised quantitative anisotropy (nQA), mean diffusivity (MD) and the principal eigenvector (V1) with the colours red, green and blue representing diffusion in x, y and z directions, and the intensity scaled by QA.

Figure 2. Scatter plot with linear fit (and 95% CI) showing the relationship between Fractional Anisotropy of the ulnar nerve in volunteers and patients, at different positions within the upper limb.

Figure 3. Scatter plot with linear fit (and 95% CI) showing the relationship between Radial Diffusivity of the ulnar nerve in volunteers and patients, at different positions within the upper limb.

Proc. Intl. Soc. Mag. Reson. Med. 29 (2021)
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